Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide
The conjugate addition of (R)-N-methyl-N-α-methylbenzyl amide to tert-butyl cinnamate followed by an asymmetric aldol reaction and subsequent N-oxidation/Cope elimination affords β-substituted homochiral Baylis-Hillman products in good yield. Copyright (C) 2000 Elsevier Science Ltd.
| Príomhchruthaitheoirí: | , , , |
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| Formáid: | Journal article |
| Teanga: | English |
| Foilsithe / Cruthaithe: |
2000
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| _version_ | 1826269075563610112 |
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| author | Davies, S Smethurst, C Smith, A Smyth, G |
| author_facet | Davies, S Smethurst, C Smith, A Smyth, G |
| author_sort | Davies, S |
| collection | OXFORD |
| description | The conjugate addition of (R)-N-methyl-N-α-methylbenzyl amide to tert-butyl cinnamate followed by an asymmetric aldol reaction and subsequent N-oxidation/Cope elimination affords β-substituted homochiral Baylis-Hillman products in good yield. Copyright (C) 2000 Elsevier Science Ltd. |
| first_indexed | 2024-03-06T21:19:23Z |
| format | Journal article |
| id | oxford-uuid:40ea594a-0f7d-43d2-9ab1-1cbe1612b5cb |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-06T21:19:23Z |
| publishDate | 2000 |
| record_format | dspace |
| spelling | oxford-uuid:40ea594a-0f7d-43d2-9ab1-1cbe1612b5cb2022-03-26T14:40:37ZAsymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amideJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:40ea594a-0f7d-43d2-9ab1-1cbe1612b5cbEnglishSymplectic Elements at Oxford2000Davies, SSmethurst, CSmith, ASmyth, GThe conjugate addition of (R)-N-methyl-N-α-methylbenzyl amide to tert-butyl cinnamate followed by an asymmetric aldol reaction and subsequent N-oxidation/Cope elimination affords β-substituted homochiral Baylis-Hillman products in good yield. Copyright (C) 2000 Elsevier Science Ltd. |
| spellingShingle | Davies, S Smethurst, C Smith, A Smyth, G Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide |
| title | Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide |
| title_full | Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide |
| title_fullStr | Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide |
| title_full_unstemmed | Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide |
| title_short | Asymmetric synthesis of homochiral Baylis-Hillman products employing (R)-N-methyl-N-alpha-methylbenzyl amide |
| title_sort | asymmetric synthesis of homochiral baylis hillman products employing r n methyl n alpha methylbenzyl amide |
| work_keys_str_mv | AT daviess asymmetricsynthesisofhomochiralbaylishillmanproductsemployingrnmethylnalphamethylbenzylamide AT smethurstc asymmetricsynthesisofhomochiralbaylishillmanproductsemployingrnmethylnalphamethylbenzylamide AT smitha asymmetricsynthesisofhomochiralbaylishillmanproductsemployingrnmethylnalphamethylbenzylamide AT smythg asymmetricsynthesisofhomochiralbaylishillmanproductsemployingrnmethylnalphamethylbenzylamide |